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Ipratropium bromide - 24208-398-30 - (Ipratropium bromide)

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Drug Information of Ipratropium bromide

Product NDC: 24208-398
Proprietary Name: Ipratropium bromide
Non Proprietary Name: Ipratropium bromide
Active Ingredient(s): 21    ug/1 & nbsp;   Ipratropium bromide
Administration Route(s): NASAL
Dosage Form(s): SPRAY, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of Ipratropium bromide

Product NDC: 24208-398
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076025
Marketing Category: ANDA
Start Marketing Date: 20030331

Package Information of Ipratropium bromide

Package NDC: 24208-398-30
Package Description: 1 BOTTLE, SPRAY in 1 CARTON (24208-398-30) > 345 SPRAY, METERED in 1 BOTTLE, SPRAY

NDC Information of Ipratropium bromide

NDC Code 24208-398-30
Proprietary Name Ipratropium bromide
Package Description 1 BOTTLE, SPRAY in 1 CARTON (24208-398-30) > 345 SPRAY, METERED in 1 BOTTLE, SPRAY
Product NDC 24208-398
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ipratropium bromide
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20030331
Marketing Category Name ANDA
Labeler Name Bausch & Lomb Incorporated
Substance Name IPRATROPIUM BROMIDE
Strength Number 21
Strength Unit ug/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Ipratropium bromide


General Information